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Novel cationic aryl bithiophene/terthiophene derivatives as corrosion inhibitors by chemical, electrochemical and surface investigations

Two novel bithienyl fluorobenzamidine derivatives namely, 4-([2,2′:5′,2′′-terthiophen]-5-yl)-2-fluorobenzamidine hydrochloride salt (MA-1615), 5′-(4-amidino-3-fluorophenyl)-[2,2′-bithiophene]-5-carboxamidine dihydrochloride salt (MA-1740) were synthesized, characterized and their corrosion inhibitio...

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Autores principales: Ismail, Mohamed A., Shaban, Mahmoud M., Abdel-Latif, Ehab, Abdelhamed, Fatma H., Migahed, Mohamed A., El-Haddad, Mahmoud N., Abousalem, Ashraf S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8873503/
https://www.ncbi.nlm.nih.gov/pubmed/35210457
http://dx.doi.org/10.1038/s41598-022-06863-8
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author Ismail, Mohamed A.
Shaban, Mahmoud M.
Abdel-Latif, Ehab
Abdelhamed, Fatma H.
Migahed, Mohamed A.
El-Haddad, Mahmoud N.
Abousalem, Ashraf S.
author_facet Ismail, Mohamed A.
Shaban, Mahmoud M.
Abdel-Latif, Ehab
Abdelhamed, Fatma H.
Migahed, Mohamed A.
El-Haddad, Mahmoud N.
Abousalem, Ashraf S.
author_sort Ismail, Mohamed A.
collection PubMed
description Two novel bithienyl fluorobenzamidine derivatives namely, 4-([2,2′:5′,2′′-terthiophen]-5-yl)-2-fluorobenzamidine hydrochloride salt (MA-1615), 5′-(4-amidino-3-fluorophenyl)-[2,2′-bithiophene]-5-carboxamidine dihydrochloride salt (MA-1740) were synthesized, characterized and their corrosion inhibition properties were evaluated by electrochemical methods for carbon steel (C-steel) in 1 M HCl. Experimental investigations revealed that the inhibition effectiveness of the investigated inhibitors (INHs) by the Tafel polarization method followed the order: MA-1740 (96.9%) > MA-1615 (95.6%), demonstrating higher efficiency than inhibitors of similar structure reported in the literature. The investigated bithiophene derivatives exhibit mixed-type corrosion inhibition characteristics by blocking the active sites on the surface of C-steel. EIS study revealed that the INHs behave as interface-type corrosion inhibitors. UV–Visible spectrometric measurements confirmed a complex formation between the Fe(2+) cation released during the corrosion reactions and inhibitor molecules.
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spelling pubmed-88735032022-02-25 Novel cationic aryl bithiophene/terthiophene derivatives as corrosion inhibitors by chemical, electrochemical and surface investigations Ismail, Mohamed A. Shaban, Mahmoud M. Abdel-Latif, Ehab Abdelhamed, Fatma H. Migahed, Mohamed A. El-Haddad, Mahmoud N. Abousalem, Ashraf S. Sci Rep Article Two novel bithienyl fluorobenzamidine derivatives namely, 4-([2,2′:5′,2′′-terthiophen]-5-yl)-2-fluorobenzamidine hydrochloride salt (MA-1615), 5′-(4-amidino-3-fluorophenyl)-[2,2′-bithiophene]-5-carboxamidine dihydrochloride salt (MA-1740) were synthesized, characterized and their corrosion inhibition properties were evaluated by electrochemical methods for carbon steel (C-steel) in 1 M HCl. Experimental investigations revealed that the inhibition effectiveness of the investigated inhibitors (INHs) by the Tafel polarization method followed the order: MA-1740 (96.9%) > MA-1615 (95.6%), demonstrating higher efficiency than inhibitors of similar structure reported in the literature. The investigated bithiophene derivatives exhibit mixed-type corrosion inhibition characteristics by blocking the active sites on the surface of C-steel. EIS study revealed that the INHs behave as interface-type corrosion inhibitors. UV–Visible spectrometric measurements confirmed a complex formation between the Fe(2+) cation released during the corrosion reactions and inhibitor molecules. Nature Publishing Group UK 2022-02-24 /pmc/articles/PMC8873503/ /pubmed/35210457 http://dx.doi.org/10.1038/s41598-022-06863-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Ismail, Mohamed A.
Shaban, Mahmoud M.
Abdel-Latif, Ehab
Abdelhamed, Fatma H.
Migahed, Mohamed A.
El-Haddad, Mahmoud N.
Abousalem, Ashraf S.
Novel cationic aryl bithiophene/terthiophene derivatives as corrosion inhibitors by chemical, electrochemical and surface investigations
title Novel cationic aryl bithiophene/terthiophene derivatives as corrosion inhibitors by chemical, electrochemical and surface investigations
title_full Novel cationic aryl bithiophene/terthiophene derivatives as corrosion inhibitors by chemical, electrochemical and surface investigations
title_fullStr Novel cationic aryl bithiophene/terthiophene derivatives as corrosion inhibitors by chemical, electrochemical and surface investigations
title_full_unstemmed Novel cationic aryl bithiophene/terthiophene derivatives as corrosion inhibitors by chemical, electrochemical and surface investigations
title_short Novel cationic aryl bithiophene/terthiophene derivatives as corrosion inhibitors by chemical, electrochemical and surface investigations
title_sort novel cationic aryl bithiophene/terthiophene derivatives as corrosion inhibitors by chemical, electrochemical and surface investigations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8873503/
https://www.ncbi.nlm.nih.gov/pubmed/35210457
http://dx.doi.org/10.1038/s41598-022-06863-8
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